A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043893



Internal ID21953184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114658778..114658778hg38UCSC Ensembl
chr1:115201399..115201399hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526981
Samples
Known GenesDENND2C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043893
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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